Description: One of the primary prerequisites for the application of organic proxies is that they should not be substantially affected by diagenesis. However, studies have shown that oxic degradation of biomarker lipids can affect their relative distribution. We tested the diagenetic stability of the UK'37 and TEX86 palaeothermometers upon long term oxygen exposure. For this purpose, we studied the distributions of alkenones and glycerol dialkyl glycerol tetraethers (GDGTs) in different sections of turbidites at the Madeira Abyssal Plain (MAP) that experienced different degrees of oxygen exposure. Sediments were deposited anoxically on the shelf and then transported by turbidity currents to the MAP, which has oxic bottom water. This resulted in partial degradation of the turbidite organic matter as a result of long term exposure to oxic bottom water. Concentrations of GDGTs and alkenones were reduced by one to two orders of magnitude in the oxidized parts of the turbidites compared to the unoxidized parts, indicating substantial degradation. High-resolution analysis of the Pleistocene F-turbidite showed that the UK'37 index of long chain alkenones increased only slightly (0.01, corresponding to 〈0.5 °C) in the oxidized part of the turbidite, suggesting minor preferential degradation of the C37:3 alkenone, in agreement with previous studies. TEX86 values showed a small increase (0.02, corresponding to ~2 °C) in the F-turbidite, like UK'37 , while for other Pliocene/Miocene turbidites it either remained unchanged or decreased substantially (up to 0.06, corresponding to ~6 °C). Previous observations showed that the BIT index, a proxy for the contribution of soil organic matter to total organic carbon, was always substantially higher in the oxidized part in all the turbidites, as a result of preferential degradation of marine-derived GDGTs. This relative increase in soil-derived GDGTs affects TEX86, as the isoprenoid GDGT distribution on the continent can be quite different from that in the marine environment. Our results indicate that the organic proxies are affected by long term oxic degradation to different extents; this should be taken into account when applying these proxies in palaeoceanographic studies of sediments which have been exposed to prolonged oxic degradation.

Description: Two sediment cores from the western Arabian Sea, NIOP905 and 74KL, were analyzed to determine sea surface temperature (SST) variations over the last 23 kyr. Two organic molecular SST proxies were used, the well-established UK'37 based on long-chain unsaturated ketones synthesized by haptophyte algae and the newly proposed TEX86 derived from the membrane lipids of Crenarchaeota. Comparison of NIOP905 and 74KL core top data with present-day SST (0-10 m) values indicates that both proxies yield temperatures similar to local annual mean SSTs. However, TEX86 and UK'37 SST down-core records derived from the same cores differ in magnitude and phasing. The alkenone SST record of NIOP905 shows small changes in SST (~0.5°C) over the last 23 kyr, while that of core 74KL shows a ~2°C increase from the Last Glacial Maximum (LGM) (23-19 calendar (cal) kyr B.P.) through the Holocene (the last 11.5 cal kyr B.P.) synchronous with changes in the Northern Hemisphere. In contrast, the TEX86 records of both cores show a large increase in SST from 22°-23°C in the LGM to 28°-30°C during Termination I (19-11.5 cal kyr B.P.), decreasing to present-day annual means of ~26°C. A cold phase between 14.5 and 12 cal kyr B.P. that may correspond to the Antarctic cold reversal is also observed. This implies a Southern Hemisphere control on tropical SST reconstructed by the TEX86, possibly related to SW monsoon. Our results suggest that the application of both TEX86 and UK'37 give different but complementary information on SST developments in past marine environments.